Surgical connector systems and methods of use

ABSTRACT

A system and method of use for effecting the bypass or other anastomosis, connection, or port in a portion of a native blood vessel, duct, lumen or other tubular organ within the body of a living being. The system includes a connector assembly and a deployment instrument for carrying the device to the desired position within the vessel, duct, lumen or tubular organ. The system includes a piercer-dilator instrument to form an opening in the wall of the vessel, duct, lumen or tubular organ into which a connector assembly may be deployed by the deployment instrument. The connector assembly may be at least partially formed of a resorbable material and includes movable members for securing it to the tissue of the vessel, duct, lumen or tubular organ contiguous with the opening. Other components may be included in the device for expediting the procedure, with or without the use of sutures.

RELATED APPLICATIONS

This application is a Continuation of our earlier filed U.S. patentapplication Ser. No. 11/179,456 filed Jul. 11, 2005 now U.S. Pat. No.7,264,624, which is a Continuation of our earlier filed U.S. patentapplication Ser. No. 09/497,274 on Feb. 3, 2000 now U.S. Pat. No.6,350,280, entitled Surgical Connector Systems And Methods Of Use, whichin-turn is a Continuation of our earlier filed U.S. patent applicationSer. No. 08/923,682 on Sep. 4, 1997 now U.S. Pat. No. 6,063,114,entitled Connector System For Vessels, Ducts, Lumens or Hollow OrgansAnd Methods Of Use, now U.S. Pat. No. 6,063,114, all of which areassigned to the same assignee as this invention and whose disclosuresare incorporated by reference herein.

BACKGROUND OF THE INVENTION

This invention relates generally to medical devices and methods ofperforming surgical procedures and more particularly to the anastomosisof blood vessels, ducts, lumens or other tubular organs.

Arterial bypass surgery is a common modality for the treatment ofocclusive vascular disease. Such surgery typically involves a formalsurgical incision and exposure of the occluded vessel followed by thejoinder of a graft, e.g., a mammary artery, saphenous vein, or syntheticgraft (all collectively referred to hereinafter as the “bypass graft”),to the occluded vessel—(hereinafter the “native” blood vessel) distally(downstream) of the occlusion. The upstream or proximal end of thebypass graft is secured to a suitable blood vessel upstream of theocclusion, e.g., the aorta, to divert the flow of blood around theblockage. Other occluded or diseased blood vessels, such as the carotidartery, may be similarly treated. Moreover, similar procedures areconducted to place a graft between an artery and a vein in dialysispatients.

While such surgical procedures are widely practiced they have certaininherent operative limitations. For example, sewing the graft to thehost vessel, known as anastomosis, requires complex and delicatesurgical techniques to accomplish the optimum result. Variouscomplications must be avoided when anastomosing a bypass graft, whetherit be a natural graft or a synthetic graft. For example, it is importantthat the juncture between the native vessel and the bypass graft form asmooth uniform transition without narrowing or regional irregularitieswhich could tend to reduce blood flow. Moreover, any protuberances intothe lumen could obstruct blood flow and may produce turbulence, therebyincreasing the risk of clotting and/or restenosis. In addition, thedifference in size between the typically larger internal diameter of thebypass graft and the typically smaller native artery may also produceunwanted turbulence in the blood. All of these characteristics cangreatly diminish the effectiveness and patency of the graft.

Various devices and methods of use have been disclosed for effectinganastomosis of blood or other vessels, ducts, lumens or other tubularorgans. Examples of such devices and methods are found in U.S. Pat. Nos.2,127,903 (Bowen), 3,155,095 (Brown), 3,588,920 (Wesolowski), 3,620,218(Schmitt et al.), 3,683,926 (Suzuki), 4,214,586 (Mericle), 4,233,981(Schomacher), 4,366,819 (Kasler), 4,368,736 (Kasler), 4,470,415(Wozniak), 4,501,263 (Harbuck), 4,675,008 (Tretbar), 4,512,761 (Raible),4,552,148 (Hardy, Jr. et al.), 4,721,109 (Healy), 4,753,236 (Healy),4,769,029 (Patel), 4,851,001 (Taheri), 4,816,028 (Kapadia et al.),4,854,318 (Solem et al.), 4,930,502 (Chen), 4,931,057 (Cummings et al.),4,957,499 (Lipatov et al.), 5,156,619 (Ehrenfeld), 5,123,908 (Chen),5,192,289 (Jessen), 5,250,058 (Miller), 5,222,963 (Brinkerhoff et al.),5,330,490 (Wilk et al.), 5,346,501 (Regula et al.), 5,364,389(Anderson), 5,399,352 (Hanson), 5,425,738 (Gustafson et al.), 5,425,739(Jessen), 5,443,497 (Venbrux), 5,445,644 (Pietrafitta et al.), 5,447,514(Gerry et al.), 5,456,712 (Maginot), 5,456,714 (Owen), 5,503,635 (Saueret al.), 5,509,902 (Raulerson), 5,571,167 (Maginot), 5,586,987 (Fahy)and 5,591,226 (Trerotola et al.).

In our co-pending U.S. patent application Ser. No. 08/861,584 filed onMay 22, 1997 entitled Anastomosis System And Method of Use, which isassigned to the same assignee as this invention and whose disclosure isincorporated by reference herein, there is disclosed and claimedanastomosis systems and methods of use which overcome many of thedisadvantages of the prior art.

OBJECTS OF THE INVENTION

It is a general object of this invention to provide connection, e.g.,anastomosis, systems for vessels, ducts, lumens or hollow organs, andmethods of use which furthers the state of the art.

It is a further object of this invention to provide a system and methodof use for quickly, easily and safely effecting the anastomosis ofvessels, ducts, lumens or other hollow or tubular organs.

It is a further object of this invention to provide a system and methodof use for quickly, easily and safely effecting the formation of a fluidaccess port in vessels, ducts, lumens or other hollow or tubular organs.

It is a further object of the invention to provide absorbable devicesfor effecting the anastomosis of vessels, ducts, lumens, or other hollowor tubular organs.

It is a further object of the invention to provide absorbable devicesfor effecting the formation of a fluid access port in vessels, ducts,lumens, or other hollow or tubular organs.

It is a further object of this invention to provide a connector devicefor effecting the anastomosis of vessels, ducts, lumens or other hollowor tubular organs or for forming a fluid access port in vessels, ductsor lumens and which device is arranged for quick and sure placement withminimal chance of error.

It is a further object of this invention to provide a device for joiningthe ends of interrupted tubes or tubular organs of various sizes andfunctions, including, but not limited to, arteries, veins, lymphaticducts, oviducts, ureters, intestines and the like.

It is a further object of the subject invention to provide a system forrapidly connecting two tubular bodies, e.g., a bypass graft to a nativeartery, without the need for sutures.

It is a further object of this invention to provide an instrument systemfor effecting the quick and easy insertion of an anastomosis device intoa vessel, duct, lumen or other hollow or tubular organ.

It is a further object of this invention to provide a connector devicefor forming a port in a vessel, duct, lumen or other hollow or tubularorgan.

It is a further object of this invention to provide an instrument systemfor effecting the quick and easy insertion of a connector device forforming a port in a vessel, duct, lumen or other hollow or tubularorgan.

It is a further object of this invention to provide a system foreffecting the anastomosis of a coronary bypass graft, e.g., theanastomosis of a bypass graft to the aorta, which may be accomplishedwithout stoppage of the heart.

SUMMARY OF THE INVENTION

These and other objects of the instant invention are achieved byproviding a system for effecting the bypass or other anastomosis of aportion of one vessel, duct, lumen or other hollow or tubular organwithin the body of a living being with another vessel, duct, lumen, orother tubular organ, e.g., a bypass graft. The one vessel, duct, lumenor tubular organ has a wall with an opening provided therein. The othervessel, duct, lumen or tubular organ has a free end portion.

The system comprises a positioning member, e.g, a filament, and firstconnector assembly for connecting the other vessel, duct, lumen, ortubular organ, e.g., a bypass graft, to the one vessel, duct, lumen ortubular organ, e.g., a native blood vessel, to establish a passagewayfor carrying fluid, e.g., blood, therebetween.

The first connector assembly basically comprises an anchor member and afirst connector member. The first connector member, e.g., a tubularflanged member, has a free end portion. The first connector member andthe anchor member are coupled together and to the positioning member,e.g., the filament, and are movable relative to each other.

The anchor member and the first connector member are arranged to beintroduced through the opening in the wall of the one vessel, duct,lumen or tubular organ, e.g., the aorta. The positioning member, e.g.,the filament, is arranged to move, e.g., pull, the anchor member intoengagement with tissue adjacent the opening in the wall of the onevessel, duct, lumen or tubular organ, and to move a portion of the firstconnector member into cooperative engagement with the anchor member andwith the free end portion of the first connector member extending outthrough the opening in the one vessel, duct, lumen or tubular organ. Thefree end of the first connector member is arranged to be secured to theother vessel, duct, lumen or tubular organ (e.g., includes means toengage cooperating means mounted on the free end of the other vessel,duct, lumen or tubular organ) to secure the two vessels, ducts, lumensor tubular organs together.

In accordance with one preferred aspect of this invention the systemincludes a deployment instrument, e.g., a carrier tube holding the firstconnector member, the anchor member and the filament, and a guide/pushermember, for introducing the first connector member and the anchor memberthrough the opening in the vessel, duct, lumen or tubular organ and forpositioning it so that it is fixedly mounted therein, with the free endof the first connector member extending out of the opening in thatvessel, duct, lumen or tubular organ.

In accordance with another aspect of this invention the first connectorassembly also includes a second connector member for securement to thefree end of the other vessel, duct, lumen or tubular organ, e.g., thebypass graft. The second connector member is arranged to be connected tothe first connector member to secure the two vessels, duct, lumens ortubular organs together.

In accordance with another preferred aspect of the invention, the firstconnector assembly can be used to form a fluid access port in the onevessel, duct, lumen or tubular organ.

DESCRIPTION OF THE DRAWINGS

Other objects and many of the attendant advantages of this inventionwill become readily appreciated as the same becomes better understood byreference to the following detailed description when considered inconnection with the accompanying drawing wherein:

FIG. 1 is a longitudinal sectional view of one embodiment of a firstconnector assembly and a deployment instrument which form a portion ofthe connector system of this invention for creating a fluid access portin a vessel, duct, lumen or tubular organ or for effecting theanastomosis between two vessels, ducts, lumens or tubular organs withinthe body of a living being;

FIG. 2 is a longitudinal sectional view of a piercing instrument and anintroducer sheath also forming a portion of the connector system of thisinvention shown during the process of forming a small opening in thewall of the vessel, duct, lumen or tubular organ;

FIG. 3 is an enlarged, isometric view of the embodiment of the connectorassembly of FIG. 1 shown in its “stowed” state disposed within thedeployment instrument of this invention prior to its deployment;

FIG. 4 is an enlarged isometric view, similar to FIG. 3, but showinganother embodiment of a connector assembly constructed in accordancewith this invention and shown in its “stowed” state prior to itsdeployment;

FIG. 5 is a longitudinal sectional view showing yet another embodimentof a connector assembly constructed in accordance with this inventionshown in its compact or “stowed” state prior to its deployment;

FIG. 6 is a longitudinal sectional view, similar to FIG. 5, but showingthe embodiment thereof in its deployed state extending through anopening in the wall of a vessel, duct, lumen or tubular organ;

FIG. 7 is a longitudinal sectional view of the introducer sheath shownin FIG. 2 extending into an opening formed within a vessel, duct, lumenor tubular organ;

FIG. 8 is a longitudinal sectional view, similar to FIG. 7, but showingthe deployment instrument extending through the introducer sheath todeploy the connector assembly of FIG. 1 into the interior of the vessel,duct, lumen or tubular organ;

FIG. 9 is an isometric view of the connector assembly of FIG. 1, shownbeing assembled in its “deployed” state;

FIG. 10 is a longitudinal sectional view of the connector assembly ofFIG. 1 shown during the deployment thereof in the opening in the wall ofthe vessel, duct, lumen or tubular organ;

FIG. 11 is a longitudinal sectional view of another connector componentforming another portion of the connector assembly of FIG. 1 and with asecond vessel, duct, lumen or tubular organ secured thereto for formingan anastomotic connection between the two vessels, ducts, lumens ortubular organs;

FIG. 12 is a longitudinal sectional view of the deployment instrument ofFIG. 1 showing the formation of the anastomosis connection between thetwo vessels, ducts, lumens or tubular organs;

FIG. 13 is an enlarged longitudinal sectional view of the distal end ofthe deployment instrument of FIG. 12 during the anastomosis connectingprocedure; and

FIG. 14 is a longitudinal sectional view showing the completedanastomotic connection between the two vessels, ducts, lumens or tubularorgans.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

Referring now to the drawing wherein like reference characters refer tolike parts, there is shown at 20 in FIG. 1 a connector systemconstructed in accordance with the subject invention.

Referring now to the various figures of the drawing wherein likereference characters refer to like parts, there is shown at 20 in FIG. 1a connector system constructed in accordance with the subject invention.The system can be used to effect the anastomosis of any two vessels,ducts, lumens or tubular organs. In fact, the system 20 can be used toform a fluid access port in any vessel, duct, lumen or tubular organ.

One particularly useful anastomosis application of the subject system isfor effecting the bypass of an occluded coronary artery. This may beaccomplished by forming an anastomotic connection between a saphenousvein graft and the aorta upstream of the occluded coronary artery. Thecompleted anastomotic connection between the bypass graft and the aortais shown in FIG. 14, wherein the bypass graft is designated by thereference numeral 10 and the aorta by the reference numeral 12.

The system basically comprises a first connector assembly 22 (FIGS. 1and 14), a deployment instrument 24 (FIGS. 1 and 12), a piercer-dilatorinstrument 26 (FIG. 2) and an introducer sheath 28 (FIGS. 2 and 7). Thedeployment instrument 24 will be described in considerable detail later.Suffice it for now to state that the instrument 24 is arranged to housea portion of the connector assembly 22 therein and to deploy it withinan opening formed in the wall of the vessel, duct, lumen or tubularorgan so that a fluid access port or an anastomosis connection can becompleted. As will also be described later, the deployment instrument 24is arranged to be used after the piercer-dilator instrument (or someother means not shown) has formed a small opening 14 (FIG. 2) in thewall of the vessel, duct, lumen or tubular organ 12 to which the fluidaccess port or anastomosis connection is to be made and the introducersheath 28 has been located within that opening.

Before describing the details of the piercer-dilator instrument 26, abrief description of the introducer sheath 28 is in order. To that end,as can be seen best in FIG. 7, the introducer sheath is of generallyconventional construction and includes an elongated tubular body 30,e.g., an 8-14 French tube. The tubular body is formed of a biocompatiblematerial, such as plastic, and has an open distal end 32 and closedproximal end 34. The proximal end 34 is closed by means of aconventional hemostasis valve housing including a resilient valve member36 disposed therein. A sealing cap 38 holds the valve member 36 in placeand includes a central opening 40 through which any suitable elongatedmember or instrument can be passed through the valve member 36 and theassociated tube 30. As will be described hereinafter the piercer-dilator26 is extended through the introducer sheath 28 and those two devicesare used together to form the small opening 14 in the vessel, duct,lumen or tubular organ. Once the opening 14 has been formed, thepiercer-dilator is removed from the sheath 28 and the introducerinstrument 24 with the connection assembly 22 therein is passed throughthe introducer sheath to deploy the connector assembly. In order toprevent excessive penetration of the piercer-dilator into the vessel,duct, lumen or tubular organ during the formation of the opening 14 inthe wall thereof, the introducer sheath 28 includes an annular stop 42closely adjacent its open distal end 32.

Turning now to FIG. 2, the details of piercer-dilator 26 will now bedescribed. Thus, as can be seen therein, the piercer-dilator 26basically comprises an elongated tubular body having a tapered distalend 44. A central passageway 46 extends down the entire length of thebody 44. A needle-plunger 48 extends through the passageway andterminates at its distal end in a sharply pointed tip 50. The proximalend of the needle-plunger is in the form of an enlarged head or cap 52.A cup shaped member 54 is mounted on the proximal end of the tubularbody 44 of the piercer-dilator 26. The cup shaped member 54 includescentral bore recess 56 arranged to receive one end of a helicalcompression spring 58. The other end of the helical spring engages theunder surface of the cap 52. The spring is normally in its uncompressedstate. It is shown in FIG. 2 in its compressed state, i.e., the statewherein the plunger cap 52 is pressed in the distal direction withrespect to the cup shaped member 54. This action causes the piercingpoint 50 of the plunger to extend out of the opening at the tapereddistal end of the dilator body 44. It is in this condition that thepiercer-dilator is used to form the small opening 14 in the wall of thevessel, duct, lumen or tubular organ to which the access port oranastomosis connection is to be made. To that end, the piercer-dilator26 is introduced through the hemostasis valve in the introducer sheath28 until its distal end extends slightly beyond the open free end 32 ofthe sheath 28. A stop (not shown) is provided to ensure that the tip ofthe needle-dilator body does not extend too far beyond the open end ofthe sheath. With the needle-dilator in place the plunger cap 52 ispressed, i.e., moved distally with respect to the body of thepiercer-dilator, whereupon the piercing point 50 extends out of thepiercer-dilator. The exposed pointed tip 50 of the piercer-dilatorinstrument is then brought into engagement with the outer surface of thevessel, duct, lumen or tubular body, e.g., the aorta 12, at which theopening 14 is to be formed. The introducer sheath and thepiercer-dilator are then pushed distally in through the wall of thevessel, duct, lumen or tubular organ, whereupon a small opening isformed. Further pushing of the needle-dilator into the opening enlargesit as the flared conical surface of the distal free end of the dilatorbody 44. Further pushing in the distal direction on the piercer-dilatorinstrument 26 and the introducer sheath 28 as a unit causes the distalend of the introducer sheath to enter into the opening 14. The combinedpiercer-dilator instrument and the introducer sheath are pushed inwarduntil the stop 42 engages the outer surface of the wall of the vessel,duct, lumen or tubular organ. At this point, no further penetration canbe made. Thus, the stop prevents the piercing tip from engaging the wallof the vessel, duct or lumen opposite the opening 14. Once the openinghas been formed, the piercer-dilator 26 can then be removed byretracting or pulling on it proximally to withdraw it out of theintroducer sheath 28 while leaving the introducer sheath in place, suchas shown in FIG. 7. The system 20 is now ready for the use of thedeployment instrument 24 to deploy the connector assembly 22 through theopening 14 into the interior of the vessel, duct, lumen or tubularorgan.

Before describing the details of the deployment instrument 24, adescription of the connector assembly 22 is in order given. To that end,as can be seen clearly in FIGS. 1, 3, 9 and 11, the connector assembly22 basically comprises a first connector member 60, an anchor member 62and a second connector member. The first connector member and the anchormember are arranged to be deployed within the interior of the vessel,duct or lumen and then to be moved with respect to each other toassemble them in a manner whereupon the anchor member engages theinterior of the vessel, duct, lumen or tubular organ contiguous with theopening 14 and a portion of the first connector member extends outthrough the opening 14 to provide a fluid access port or a connectionpoint for the second connector member 64. In some applications, thefirst connector member and the anchor member can be used in and ofthemselves to form a fluid access port to the interior of the vessel,duct, lumen or tubular organ.

As can be seen clearly in FIG. 3, the first connector member 60 and theanchor member 62 are coupled together by a positioning member, e.g., aflexible filament 66. The filament is preferably in the form of aconventional resorbable monofilament suture (or if desired anon-resorbable suture).

The anchor member 62 is an elongated strip formed of a resorbable,somewhat rigid material, such as polyglactide, polyglycolide orcopolymers thereof. Non-absorbable materials, e.g., stainless steel, canbe used for the anchor member. Each end of the anchor member 62 isrounded at 70. The first connector member 60 basically comprises atubular body, preferably formed of the same material as that forming theanchor 62, and having a central passageway 72 extending therethrough.One end of the tube 74 is in the form of an annular flange. The flangeneed not be annular, and thus may merely be a tab or projection. Theother end of the tube is in the form of at least one undercut annularlip or detent 76 whose exterior surface is chamfered. The outer surface78 of the tubular connector body 60 between the flange 74 and the detent76 is somewhat conical, i.e., is in the form of a surface which tapersfrom the flange 74 to the detent 76. The maximum outer diameter of thedetent 76 of the connector member 60 is just slightly larger than theinside diameter of the hole 68 in the anchor member 62. A small aperture80 extends radially outward from the central passageway 72 of the firstconnector member 60 through the annular flange 74.

As best seen in FIGS. 1 and 3, the filament 66 includes a pair ofsequentially located sections 66A and 66B. In particular, section 66Aextends from the proximal end of the deployment instrument 24 down theinterior of that instrument through the central opening 68 in the anchormember 60, through the central passage 72 in the first connector member60 from whence it doubles back to merge with the filament section 66B.The section 66B extends through the aperture 80 back into the interiorpassageway 72 in the first connector member 60 and through the centralopening 68 in the anchor member 62. From there the section 66B of thefilament 66 extends in the proximal direction through the deploymentinstrument to the proximal end thereof.

As mentioned earlier, the details of the deployment instrument will bedescribed later, suffice it for now to state that this instrumentincludes a carrier 82 in the form of a tubular body in which the anchormember 62 and the first connector member 60 of the connector assembly 22are disposed. The carrier tube includes an open, free (distal) end 84.As can be seen in FIGS. 1 and 3, the first connector member 60 isdisposed within the carrier tube 82 immediately adjacent the open distalend 84, while the anchor member 62 is disposed immediately proximally ofthe first connector member.

The deployment instrument 24 also includes a guide-pusher assemblylocated within the carrier tube. The guide pusher assembly includes atubular guide-pusher member 86 having a conical distal portion end 88.The free end 90 of the guide-pusher member includes a small openingcommunicating with the hollow interior of the guide-pusher and throughwhich the filament sections 66A and 66B extend. The end 90 of the pushermember 86 is located immediately adjacent the proximally located roundeddistal end 70 of the anchor member 62, when the anchor member is withinthe carrier tube in place as shown in FIGS. 1 and 3.

Deployment of the first connector member 60 and anchor member 62 isaccomplished by operating the guide-pusher assembly, as will bedescribed later, to cause the guide-pusher member 86 to push on theproximal end portion 70 of the anchor member 62 which in turn pushes onthe distally located connector member 60 to expel the first connectormember 60 out of the open free end 84 of the carrier member and out ofthe open end 32 of the introducer sheath 28 into the interior of thevessel, duct, lumen or tubular organ. Continued pushing on the guidepusher 86 in the distal direction then ejects the anchor member 62 intothe interior of the vessel, duct, lumen or tubular organ.

In order to assemble the first connector member and anchor member andcause the detent end of the first connector member to be extendedthrough the opening 14 in the wall of the vessel, duct, lumen or tubularorgan, the two extending sections 66A and 66B of the filament 66 areretracted in the proximal direction, by means forming a portion of theinstrument 24 to be described later. In particular, this retractionaction on the filament sections pulls the first connector member towardthe anchor member, whereupon the chamfered surface 76 of the firstconnector member enters into the central opening 68 in the anchormember. Continued refraction on the filament causes the anchor member toengage the interior surface of the vessel, duct, lumen or tubular organcontiguous with the opening 14 with the central opening 68 in the anchormember overlying the opening 14. Continued retraction of the twofilament sections pulls the first connector member further into thecentral opening 68 in the anchor member, whereupon the portions of theanchor member contiguous with the central opening ride up the surface 78of the first connector member until the flange 74 of the first connectormember abuts the distally directed top surface of the anchor member 62,as shown in FIGS. 9 and 10. The retraction of the first connector memberthrough the central opening 68 in the anchor member 62 causes thechamfered proximal end of the first connector member to pass through theopening 14 in the wall of the vessel, duct, lumen or tubular organ 12,as shown in FIG. 10. During the refraction of the filament sections 66Aand 66B, the guide-pusher member 86 remains stationary so that itstapered distal end 88 enters into the central passageway 72 of the firstconnector member 60 when the first connector member is pulled throughthe opening 14 in the wall of the vessel, duct, lumen or tubular organ.Thus, the tapered end of the guide-pusher member 86 serves to guide ororient the first connector member 60 so that its central longitudinalaxis is disposed generally perpendicularly to the wall of the vessel,duct, lumen or tubular organ 12, as shown in FIG. 10.

With the first connector member 60 and the anchor member 62 deployed asshown in FIG. 10, the system is now ready to complete the anastomosis.To that end, the second connector member 64 is pre-mounted on the distalend of any desired vessel, duct, lumen or tubular organ like that shownin FIG. 11. For example, as shown in FIG. 11, the connector 64 can bedisposed and secured within the open distal end of a saphenous veinbypass graft 10. The second connector member basically comprises ahollow tubular member, formed of the same material as that of the firstconnector 60 and the anchor member 62. The distal end of the secondconnector 64 is in the form of an annular flange 92. The outer surfaceof the tubular connector 64 proximally of the flange 92 is in the formof a slightly outwardly tapering conical surface 94, i.e., a surfacewhose diameter increases linearly in the proximal direction. A centralpassageway 96 extends through the length of the connector member 64, theproximal end of the passageway 96 forms a flared throat 98. Threeannular undercut detent rings 100, 102 and 104 extend about theinter-periphery of the central passageway 96 at closely spaced locationsadjacent the flanged distal end 92 of the connector 64. The outersurface of each of these detents is chamfered and is arranged tocooperate and engage the chamfered surface of the detent 76 of the firstconnector member 60 to lock the two connector members together, as willbe described later. The flared proximal end of the second connector 64is located within the hollow interior lumen of the bypass graft 10 andis secured in place therein by plural stainless steel springs 106. Thesprings extend about the periphery of the distal end of the bypass graftto interpose that portion of the bypass graft tightly between thesprings and the exterior surface 94 of the second connector member 64.Thus, the second connector member is fixedly secured to the distal endof the bypass graft.

The bypass graft with the second connector member fixedly securedthereto as shown in FIG. 11 is arranged to be deployed or slid down overthe deployment instrument 24, as will be described later, and over theguide-pusher member 86 like shown in FIG. 13, whereupon the flange 92 ofthe second connector member 64 abuts the exterior surface of the vessel,duct, lumen or tubular organ contiguous with the opening 14 therein. Theundercut surface of the detent surface 76 of the first connector memberengages one of the undercut surfaces of the three chamfered detent rings100, 102 or 104, with the particular detent being engaged beingdependent upon the thickness of the wall of the vessel, duct, lumen ortubular organ.

In the embodiment shown in FIG. 13, the undercut portion of the detent76 of the first connector member 60 engages the undercut portion of thedetent ring 102 of the second connector member 64. This actioneffectively sandwiches the wall of the vessel, duct, lumen or tubularorgan between the flange 92 of the second connector member 64 and theanchor member 62, thereby fixedly securing the connector assembly 22 inplace within the opening 14, thereby completing the anastomosis.

In accordance with a preferred embodiment of this invention, a washer108 is interposed between the flange 92 of the second connector member64 and the outer surface of the wall of the vessel, duct, lumen ortubular organ contiguous with the opening 14 to prevent bleeding at theinterface of the connector assembly and the opening 14 in the wall ofthe vessel, duct, lumen or tubular organ. The washer is preferablyformed of a hemostatic material, e.g., collagen.

As should be appreciated from the previous discussion, the embodiment ofthe connector assembly 22 described heretofore makes use of componentswhich are coupled together, but not assembled. By that it is meant thatthe components are disposed with respect to each other so that they areheld in a compact configuration within the carrier tube for expulsioninto the interior of the vessel, duct, lumen or tubular organ. Onceexpelled they are movable or positionable with respect to each other andwith respect to the wall of the vessel, duct, lumen or tubular organ toassemble them in their “deployed state.” In the deployed state theportions are oriented with respect to each other so that they areresistant to accidental dislodgement within the opening in the wall ofthe vessel, duct, lumen or tubular organ. In particular, the anchormember, lying against the interior wall of the vessel, duct, lumen ortubular organ contiguous with the opening prevents the deployedconnector assembly from falling out of that opening.

In FIG. 4 there is shown an alternative embodiment of a connectorassembly 222 constructed in accordance with this invention. The assembly222 is similar in many respects to the connector assembly 22, but inother ways differs. In this connection, the connector assembly 222includes components which are preassembled so that they are connected toeach other prior to deployment. These preassembled components are heldin a compact or “stowed” state within the carrier tube 82 so that theycan be ejected from the carrier tube as a unit into the interior of thevessel, duct, lumen or tubular organ. Once ejected, the connectorassembly 222 can then be refracted in a similar manner to that describedheretofore to bring a portion of it into engagement with the wall of thevessel, duct, lumen or tubular organ contiguous with the opening 14while another portion extends out to that opening for connection to thesecond connector member 64. The connector assembly 222 basicallycomprises a first connector member 224, an anchor member 62 and a secondconnector member 64. The anchor member 62 and the second connectormember are identical to those components making up the connectorassembly 22. Thus, in the interest of brevity, the details of the anchorcomponent 62 and the second connector component 64 will not bereiterated and the various portions of these components will be giventhe same reference numerals as given previously.

The first connector member 224 is preferably formed of the same materialas that of the anchor member 62. Moreover, the first connector member224 includes various portions which are constructed similar to theconnector member 60 of connector assembly 22. Thus, in the interest ofbrevity, the portions of the first connector assembly 224 which aresimilar to those portions of the first connector 60 will be given thesame reference numerals. In particular, the first connector member 224is a tubular member having a central passageway 72 extending through it.The distal end of the connector member 224 is in the form of an annularflange 84 while the proximal end is in the form of a chamfered surfacedetent 76. The outer surface of the connector between the flange 84 andthe detent 76 is of circular profile and extends through the centralopening 68 in the anchor member 62 so that the connector member 224 isslidable longitudinally within that opening. The connector assembly 222is arranged to be disposed in a compact or “stowed” position within thecarrier tube 82 of the deployment instrument. In particular, theconnector 224 is centered within the opening 68 in the anchor 62, asshown in FIG. 4 to ensure that it has the smallest cross sectionalprofile for disposition within the carrier tube.

A pair of apertures 226 extend radially inward through the flange 84 toenable the filament 66 to be coupled to the connector member 224. Inparticular, the filament section 66B extends through the open proximalend of the central passage 72 of the connector member 224 and outthrough one of the apertures 226. The filament section 66B extends intothe other aperture 226. From that point, the filament section 66Bextends through the passageway 72 and out the proximal end thereof. Theproximal end portions of filament sections 66A and 66B extend throughthe guide-pusher and through the deployment instrument, as will bedescribed later.

Deployment of the connector assembly 222 is accomplished in a similarmanner to that of connector assembly 22. In this regard, theguide-pusher assembly is used to push the assembled connector 224 andanchor 62 out of the carrier tube so that the preassembled connectormember 24 and the anchor member 62 are located within the interior ofthe vessel, duct, lumen or tubular organ. Retraction of the filamentsections 66A and 66B brings the proximal end of the connector member 224back through the opening 14 in the wall of the vessel, duct, lumen ortubular organ. Moreover, retraction of the filament sections causes thetop or proximal surface of the anchor member 62 to move into engagementwith the inner surface of the vessel, duct, lumen or tubular organcontiguous with the opening 14, thereby causing the anchor member to“hang-up” on that surface. Further, retraction of the filament sectionsmoves the connector member 224 with respect to the anchor member, i.e.,it causes the connector member to slide through the hole 68 in theanchor member, so that more of the connector member 224 extends out ofthe opening in the wall of the vessel, duct, lumen or tubular organuntil its flange 84 engages the bottom or distal surface of the anchormember contiguous with the hole 68. At this time, the connector device224 is fully deployed and ready for connection to the connector member64 and the bypass graft 10 connected to that connector. That connectionis accomplished in the same manner as with the connector assembly 22described earlier.

In FIG. 5, there is shown another alternative embodiment 32 of aconnector assembly constructed in accordance with this invention. Theconnector assembly 322 is somewhat similar to the connector assembly 222in that it is preassembled, i.e., its first connector and anchorcomponents are assembled or connected to each other, but are movablerelative to each other during the deployment procedure. In the interestof brevity, the common components of the connector assembly 322 andconnector assembly 222 and connector assembly 22 will be given the samereference numerals and the details of their construction and operationwill not be reiterated.

Thus, as can be seen in FIG. 5, the connector assembly 322 basicallycomprises a first connector member 324 and an anchor member 326. Thefirst connector member 324 and the anchor member 326 are an integralunit, with the anchor unit 326 being similar in construction to theanchor member 62. Thus, the anchor member includes a central hole 68.The first connector member 324 is a collapsible, e.g., a corrugated,tube having a central passageway 72 extending therethrough. The distalend of the corrugated tube 324 is in the form of a flange 328 which isreceived within a correspondingly shaped annular recess 330 extendingabout the hole 68 in the anchor member 326. The tube 324 is arranged tobe held in its compact or “stowed” state as shown in FIG. 5 when it iswithin the carrier tube of the deployment instrument, and to be extendedto its deployed state, as shown in FIG. 6, during its deployment.

The proximal end of the collapsible corrugated tube 324 is in the formof an annular collar 332 forming a detent having a chamfered surface 76.The collar 332 is fixedly secured to the proximal end of the corrugatedtube 324.

The anchor member 326 is preferably formed of a resorbable material,like that of the anchor members described heretofore. The corrugatedtube may also be formed of the same resorbable material. Alternatively,it may be formed of any conventional biocompatible material, such asDacron mesh, providing that it is impervious to the flow of liquidthrough it so that fluid flowing through the central passageway 72 willnot leak out the wall of the corrugated tube 324 much like a syntheticvascular graft.

A radially oriented aperture 334 is provided in the annular collar 332through which the filament 66 extends so that one filament section 66Bextends from one side of the aperture while the other filament section66A extends from the other.

The connector assembly 322 is disposed within the carrier tube 82 in itscompact state like that shown in FIG. 5, so that its anchor member isoriented parallel to the central longitudinal axis of the carrier tubeand immediately distally of the distal end 90 of the guide-pusher member86. The filament sections 66A and 66B extend back through the interiorof the guide-pusher and through the deployment instrument. The connectorassembly 322 is ejected from the carrier tube in the same manner asdescribed with reference to the connector assemblies 22 and 222. Onceejected into the interior of the vessel, duct, lumen or tubular organ,the two filament sections 66A and 66B are retracted. As will bedescribed later, to draw the collar 332 of the connector assembly 332back through the opening 14 in the wall of the vessel, duct, lumen ortubular organ. Continued retraction of the filament sections cause thetop or proximal surface of the anchor member 326 to engage the interiorsurface of the vessel, duct, lumen or tubular organ contiguous with theopening 14 to cause it to hang-up in the same manner as describedearlier. Once the anchor hangs-up, continued retraction of the filamentsection cause the corrugated tube 324 to stretch or straighten out,thereby increasing the length of the tube from the state shown in FIG. 5to the state shown in FIG. 6. Once the connector assembly 322 is in thefully deployed state shown in FIG. 6, the second connector member 64 andthe bypass graft 10 connected to it can be secured to the assembly 322in the same manner as described heretofore.

Referring now to FIGS. 1 and 12, the details of the deploymentinstrument 24 will now be described. Thus, as can be seen the deploymentinstrument 24 basically comprises the heretofore identified carrier tube82 and the heretofore described pusher-guide assembly. That assemblyincludes the pusher-guide member 86 and an actuation assembly 110.

The carrier tube 84 includes an annular ring or stop 112 secured aboutis outer periphery immediately adjacent the proximal end 114. The stop112 is provided to ensure that the carrier tube of the deploymentinstrument is not extended too far into the introducer sheath 28. Thus,the stop is arranged to engage the rear wall 38 of the hemostasis valvewhen it is in proper position.

The proximal end 114 of the guide tube is in the form of an inwardlyextending, annular wall 116 having a central passageway 118 therein. Thepassageway 118 is adapted to closely receive the outer surface of thecylindrical portion of the pusher-guide member 86 to form a generallyfluid-tight seal therebetween. The proximal end 120 of the pusher-guidemember 86 is in the form of an inwardly extending annular wall 122having a central passageway 124 therein. The central passageway 124 isarranged to closely receive a portion of the actuation assembly 110 (tobe described hereinafter) to form a generally fluid tight sealtherebetween.

The actuation assembly 110 basically comprises an elongated cylindricalmandrel rod 126 having a central passageway 128 extending along itslength between its open distal end 130 and its open proximal end 132.The passageway 128 communicates with the interior of the pusher-guidemember 86. An actuation cap 134 is mounted on the proximal end of themandrel rod, with a helical compression spring 136 extends about theouter periphery of the hollow mandrel rod 126 interposed between theproximal end 120 of the pusher-guide tube 86 and a stop surface 138forming the distal end of the actuation cap 134. The cap 134 basicallycomprises a pair of hollow tubular sections 140 and 142. The section 142is disposed proximally of section 140 and is cup-shaped. The section 140is fixedly secured to the mandrel rod 126 with the distal end of thefilament section 66B tightly interposed therebetween. In particular,filament sections 66A and 66B extend from the connector assembly 22through the pusher-guide member 86 into the hollow interior of themandrel rod 126 and out the proximal end opening 132 of the passageway128 extending through the mandrel rod 126. The distal end portion offilament 66B extends under the cup-shaped cap section 142 and is trappedbetween the outer surface of the mandrel rod 126 and the inner surfaceof the cap shaped 140. The distal end of the filament section 66A alsoextends out the proximal end 132 of the passageway 128 and is trappedbetween the outer surface of the mandrel tube 128 and the inner surfaceof the cup-shaped portion 142 of the cap 134. The cup-shaped portion 142of the cap is removable for reasons to be described later.

The cap 134 also includes a central aperture in its end wall incommunication with the interior passageway 128 of the mandrel tube 126.A plug, formed of a resilient material, such as rubber, is releasablylocated within the aperture 144 to seal it. The aperture 144, with theplug removed serves as a means to enable the deployment instrument 24 todetermine the location of the wall of the vessel, duct, lumen or tubularorgan as will be described later.

Operation of the deployment instrument 24 is as follows:

The instrument is inserted into the introducer sheath after the sheathhas been positioned with the piercer-dilator to form the opening 14 inthe wall of the vessel, duct, lumen or tubular organ and thepiercer-dilator has been removed. To that end, the deployment instrumentis extended through the introducer sheath which is positioned as shownin FIG. 7 until the stop ring 112 on the deployment instrument 24 abutsthe proximal end 38 of the hemostasis valve of the introducer sheath 28,as shown in FIG. 8. The cap 134 of the actuation assembly 110 is thenpushed in the distal direction, thereby imparting movement in the distaldirection to the pusher-guide tube 86 via the interposed spring 136.This action causes the free distal end 90 of the guide-pusher member toengage the proximal end of the anchor member 64 of the connectorassembly 22 within the carrier tube 82. Continued pushing on the cap inthe distal direction causes the pusher-guide member to eject the firstconnector member 60 and the anchor member 62 as described heretofore.Once the connector assembly's components are free of the guide tube andare located within the interior of the vessel, duct, lumen or tubularorgan, the spring in attempting to assume its uncompressed naturalstate, applies tension to the filament sections 66A and 66B. Inparticular, the release of pressure on the cap 136 allows the spring tomove from its compressed state shown in FIG. 1 to a longitudinallyexpanded or uncompressed state shown in FIG. 12. Since the filament endsare trapped by the cap 134, this action pulls the filament sections inthe proximal direction, thereby drawing the components 60 and 62 of thefirst connector assembly 22 into the deployed state shown in FIGS. 9 and10. Once the components are in this state, the introducer sheath iswithdrawn, i.e., pulled off the instrument, leaving the deploymentinstrument 24 in the position shown in FIG. 12.

The second connector member 64 with the bypass graft 10 secured theretois then threaded and slid down the instrument 24 over the actuationassembly and the pusher-guide tube to the position shown in FIG. 12. Ifa hemostatic washer 108 is used, as is preferable, that washer isthreaded on the deployment instrument in advance of the second connectormember 64.

When the second connector member 64 and the associated bypass graft 10are slid in a distal direction until the flange 92 either directlyengages the anchor surface of the wall of the vessel, duct, lumen ortubular organ or indirectly engages it via an interposed hemostaticwasher 108. One of the chamfered detents of the second connector member64 will be engaged by chamfered detent 76 of the first connector member60 to secure the first and second connector members together.

Once the connector members 60 and 62 are connected together, thedeployment instrument 24 can be removed to leave the anastomoticconnection in position. To that end, the cup-shaped portion 142 of theactuating cap 134 is removed, thereby freeing the proximal end offilament section 66A. The remaining portion 142 of the cap 146 is thenpulled or withdrawn in the proximal direction to withdraw the deploymentinstrument from within the interior of the bypass graft 10. Since theproximal end of filament section 66A is no longer trapped but theproximal end of the filament section 66B is trapped by the cap section140 retraction of the instrument 24 causes the filament section 66A tomove down the passageway 128 of the mandrel tube. Eventually, the freeend of section 66A will pass through the aperture 80 in the firstconnector member 60 and from there will be pulled through the passageway72 of that member and through the bypass graft interior until it exitsthe proximal end of the graft. At this point, the deployment instrument24 will be fully removed from the anastomotic connection, leaving thatconnection in the state shown in FIG. 14.

The proximal end (not shown) of the bypass graft 10 can be secured tothe occluded coronary artery (not shown) distally of the occlusion byany suitable technique. For example, the distal end of the bypass graftcan be surgically connected to the coronary artery, or it can beconnected utilizing means similar to that described herein introducedvia an access port or slit (not shown) made in the wall of the bypassgraft or by means such as taught in our co-pending United States patentapplication identified above.

As mentioned earlier, the actuation cap 134 of the deployment instrument24 includes an aperture 144 which is sealed with a plug 146. Theaperture 144 enables one to determine if the deployment instrument isproperly positioned with respect to the wall of the vessel, duct, lumenor tubular organ. This action is accomplished by removing the plug 146from the aperture so if the instrument is disposed at the desiredposition it will be in communication with the interior of the vessel,duct, lumen or tubular organ. Accordingly, blood will be enabled to flowfrom the interior of the vessel, duct, lumen or tubular organ andthrough the hollow interior of the pusher-guide member, and thecommunicating passageway in the mandrel tube where it exits the proximalend of that passageway and through communicating port 144. Thus, when adrop of blood or other fluid appears at the port, the user of theinstrument 24 knows that the device is in the desired position. The plug146 can then be reinserted into the aperture 144 to seal it so that nofurther blood can gain egress through the instrument 24.

It should be pointed out at this juncture that the piercer-dilatorinstrument 26 may be constructed to utilize a similar flashbackconstruction to provide an indication of proper placement, by the egressof a drop of blood from the proximal end of the piercer-dilator. Morelikely, the formation of the opening in the wall of the vessel, duct,lumen or tubular organ will be preformed under direct vision. If a fluidflashback system is incorporated into piercer-dilator, or the introducersheath, it will allow placement of the introducer sheath at a specificlocation within the vessel, duct, lumen or tubular organ without theneed for direct observation.

It must be pointed out at this juncture that it is contemplated that theconnector assemblies of this invention could be actively assembled ordeployed by manual pulling of the filament sections and pushing on thepusher member instead of using a spring loaded system like describedheretofore.

The bypass graft 10 is prepared by inserting the proximal end of thesecond connector member 64 into the open distal end of the graft section10. The connector is held in place by use of one or more stainless steelspring clips 106. The spring clips and the second connector 64 arepreferably available in different sizes to cater to different graftsizes. In particular, the spring clips 106 are sized to a predeterminedinside diameter to limit the constriction of the graft which wouldotherwise cause necrosis of the interposed tissue due to excessivepressure. Other means can be utilized to secure the graft 10 to thesecond connector member 64. Such means may be a biocompatible adhesive,pre-knotted suture loops, sutures, c-clips, etc.

The inside profile of the passageways of the connector assemblies ofthis invention are preferably designed to minimize turbulence andcontrol the pressure of fluid flowing therethrough, such as disclosed inour heretofore identified co-pending patent application. It should alsobe pointed out that the various connector components of the connectorassemblies of this invention can be coated with, or impregnated withchemicals, drugs, or other biologically active components to affect thenearby tissue or cells. Such active components could include, but arenot limited to, anti-platelet drugs, antimicrobial agents, antibiotics,anti-thrombogenic materials, anti-oxidants, growth factors, growthhormones, genetic material, or seeded cells.

It should be noted that the embodiments of the connector assembliesand/or the deployment instrument and/or the piercer-dilator instrument,and/or the introducer sheath as shown and described heretofore aremerely exemplary. Thus, other constructions are contemplated. Forexample, the anchor member may be shaped other than a linear strip,e.g., it may be slightly arcuate or trough-shaped like that disclosed inour aforementioned copending application. The positioning member for theconnector assemblies may comprise other types of components making useof at least one filament or may comprise other devices, such as aflexible wire having a balloon on its distal end. The connectorassemblies and/or the components thereof need not be formed to betotally resorbable. Thus, none or only portions of such assemblies maybe resorbable.

Without further elaboration the foregoing will so fully illustrate ourinvention that others may, by applying current or future knowledge,adopt the same for use under various conditions of service.

1. A system to effect a port, connection, or anastomosis of a portion ofa blood vessel, duct, lumen or other tubular organ in the body of aliving being by use of a connector assembly, said system comprising (i)a piercer-dilator instrument, (ii) an introducer sheath, and (iii) adeployment instrument, (a) wherein said piercer-dilator instrumentcomprises a proximal end and a distal end, and said piercer-dilatorinstrument is configured to form a small opening in the blood vessel,duct, lumen or other tubular organ to allow for the introduction of saidintroducer sheath, (b) wherein said introducer sheath comprises aproximal end, a distal end, and a hemostasis valve to atop flow of afluid comprising blood, with said introducer sheath being arranged tofacilitate introduction of said deployment instrument, (c) wherein saiddeployment instrument comprises said connector assembly, wherein saidconnector assembly comprises at least a first connecting member and ananchor member, with said members being arranged to be fixedly attachedto each other, and said first connecting member comprises a tubular bodyhaving a central passageway therethrough, and wherein at least a portionof said connector assembly is arranged to be deployed internal to saidblood vessel, duct, lumen or other tubular organ, thereby completingsaid port, connector, or anastomosis.
 2. The system of claim 1, whereinsaid introducer sheath has a generally tubular body.
 3. The system ofclaim 1, wherein said tubular body comprises a flange.
 4. The system ofclaim 3, wherein said flange is annular.
 5. The system of claim 4,wherein a small aperture extends radially outward from said centralpassageway of said first connecting member through said annular flange.6. The system of claim 3, wherein said anchor member defines a holetherethrough.
 7. The system of claim 6, wherein an outer diameter ofsaid flange is just slightly larger than an inside diameter of said holein said anchor member.
 8. The system of claim 3, wherein said flangecomprises a tab.
 9. The system of claim 1, wherein an end of saidtubular body opposite said flange comprises an undercut annular lip. 10.The system of claim 9, wherein an exterior surface of said undercutannular lip is chamfered.
 11. The system of claim 1, wherein an outersurface of said tubular body is conical.
 12. A system to effect a port,connection, or anastomosis of a portion of a blood vessel, duct, lumenor other tubular organ in the body of a living being by use of aconnector assembly, said system comprising (i) a piercer-dilatorinstrument, (ii) an introducer sheath, and (iii) a deploymentinstrument, (a) wherein said piercer-dilator instrument comprises aproximal end and a distal end, and said piercer-dilator instrument isconfigured to form a small opening in the blood vessel, duct, lumen orother tubular organ to allow for the introduction of said introducersheath, (b) wherein said introducer sheath comprises a proximal end anda distal end, with said introducer sheath being arranged to facilitateintroduction of said deployment instrument, wherein said introducersheath further comprises an axial passageway in communication with saidproximal and said distal ends of said deployment instrument, with saidcommunication serving to allow fluid to visibly exit said deploymentinstrument, wherein the visibly exiting fluid gives an indication oflocation within said blood vessel, duct, lumen or other tubular organ,and wherein said passageway in said introducer sheath further comprisesa cap or plug to stop the flow of said fluid, (c) wherein saiddeployment instrument comprises said connector assembly, wherein saidconnector assembly comprises at least a first connecting member and ananchor member, with said members being arranged to be fixedly attachedto each other, and said first connecting member comprises a centralpassageway arranged for flow of the fluid therethrough, and wherein atleast a portion of said connector assembly is arranged to be deployedinternal to said blood vessel, duct, lumen or other tubular organ,thereby completing said port, connector, or anastomosis.
 13. The systemof claim 12, wherein said system further comprises an annular stoplocated near said distal end of said introducer sheath.
 14. A system toeffect a port, connection, or anastomosis of a portion of a bloodvessel, duct, lumen or other tubular organ in the body of a living beingby use of a connector assembly, said system comprising (i) apiercer-dilator instrument, (ii) an introducer sheath, and (iii) adeployment instrument, (a) wherein said piercer-dilator instrumentcomprises a proximal end and a distal end, and said piercer-dilatorinstrument is configured to form a small opening in the blood vessel,duct, lumen or other tubular organ to allow for the introduction of saidintroducer sheath, (b) wherein said introducer sheath comprises aproximal end and a distal end, with said introducer sheath beingarranged to facilitate introduction of said deployment instrument, (c)wherein said deployment instrument comprises said connector assembly,wherein said deployment instrument further comprises a carrier tubehaving a proximal end and a distal end, with at least the distal endbeing open, wherein said deployment instrument further comprises apositioning member, with said first connector member and said anchorbeing disposed longitudinally in said carrier tube, prior to theirdeployment, wherein said connector assembly comprises at least a firstconnecting member and an anchor member, with said members being arrangedto be fixedly attached to each other, and said first connecting membercomprising a tubular body having a central passageway therethrough, andwherein at least a portion of said connector assembly is arranged to bedeployed internal to said blood vessel, duct, lumen or other tubularorgan, thereby completing said port, connector, or anastomosis, (d) saidsystem further comprising a pusher-guide assembly located proximal tosaid anchor and said first connector member, wherein said pusher-guideassembly comprises a pusher-guide member and an actuation assembly,wherein said pusher-guide member comprises a central passageway, whereinsaid central passageway of said pusher-guide member is arranged toreceive at least a portion of said actuation assembly.
 15. The system ofclaim 14, wherein said actuation assembly comprises a cylindricalmandrel rod having a central passageway extending along its lengthbetween open distal and open proximal ends of said rod, and whereinfurther said central passageway of said rod communicates with saidcentral passageway of said pusher-guide member, and wherein saidactuation assembly further comprises an actuation cap mounted on theproximal end of said mandrel rod.
 16. The system of claim 15, whereinsaid actuation cap comprises a proximal end and a distal end, andwherein a stop surface forms said distal end.
 17. The system of claim16, wherein said actuation assembly further comprises a helicalcompression spring extending around the outer periphery of at least aportion of said cylindrical mandrel rod, said spring being interposedbetween the proximal end of said pusher-guide member and said stopsurface of said actuation cap.